Eurotherm Data Reviewer FDA 21 CFR Part 11
●As part of an ongoing commitment to aid compliance to the US Code of Federal Regulations from the Foodand Drug Administration (FDA) and specifically FDA 21 CFR Part 11 requirements, this data sheet demonstrates how Eurotherm domain expertise helps customers meet the various requirements of FDA 21 CFR Part 11.Each subsection considered is listed in the header of the tables below, and the statements within each table are accompanied by a commentary demonstrating how the Eurotherm solution aids compliance.
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Datasheet |
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Please see the document for details |
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English Chinese Chinese and English Japanese |
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April 2020 |
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Issue 1 |
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HA033530 |
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1 MB |
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